A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3620607



Internal ID18918888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:25555425..25590273hg38UCSC Ensembl
Innerchr4:25557047..25591895hg19UCSC Ensembl
Innerchr4:25166145..25200993hg18UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg3834849
hg1934849
hg1834849
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv998697
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3620607
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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